Osler-Weber-Rendu Syndrome - Dental Implications


Autoria(s): SANTOS, Paulo Sergio da Silva; FERNANDES, Karin Sa; MAGALHAES, Marina Helena
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/04/2012

18/04/2012

2009

Resumo

Osler-Weber-Rendu syndrome (OWRS) is a rare hereditary, autosomal dominant disease characterized by a local angiodysplasia. Its clinical characteristics are vascular hamartomas of the skin and oral mucosa, arteriovenous malformations in the lungs, liver, kidney and brain, and episodes of epistaxis. The oral lesions, which become apparent through hemorrhagic telangiectasia, may be the first sign of the disease. This is a case report of a 74-year-old woman whose diagnosis of OWRS was established by her dentist based on the presence of telangiectasia in the skin and oral mucosa, reports of frequent nosebleeds of unknown etiology and a family history of telangiectasia. Amputation of a lower limb and comorbidities, such as cardiopathy, nephropathy and rheumatic disorders, completed the profile. OWRS causes major vascular changes that can be diagnosed initially by a dentist. In this article, we describe the skills and knowledge that dentists need to monitor patients with OWRS properly.

Identificador

JOURNAL OF THE CANADIAN DENTAL ASSOCIATION, v.75, n.7, p.527-530, 2009

1488-2159

http://producao.usp.br/handle/BDPI/15459

http://www.cda-adc.ca/jcda/vol-75/issue-7/527.pdf

Idioma(s)

eng

Publicador

CANADIAN DENTAL ASSOC

Relação

Journal of the Canadian Dental Association

Direitos

openAccess

Copyright CANADIAN DENTAL ASSOC

Palavras-Chave #HEREDITARY HEMORRHAGIC TELANGIECTASIA #PULMONARY ARTERIOVENOUS-MALFORMATIONS #BRAIN-ABSCESS #DISEASE #MANIFESTATIONS #UPDATE #Dentistry, Oral Surgery & Medicine
Tipo

article

original article

publishedVersion